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Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma
The iliac crest is the sampling site for minimal residual disease (MRD) monitoring in Multiple Myeloma (MM). However, the disease distribution is often heterogeneous, and imaging can be used to complement MRD detection at a single site. We have investigated patients in complete remission (CR) during...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586541/ https://www.ncbi.nlm.nih.gov/pubmed/30573775 http://dx.doi.org/10.1038/s41375-018-0329-0 |
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author | Rasche, L Alapat, D Kumar, M Gershner, G McDonald, J Wardell, C.P Samant, R Van Hemert, R Epstein, J Williams, A.F Thanendrarajan, S Schinke, C Bauer, M Ashby, C Tytarenko, R.G van Rhee, F Walker, B.A Zangari, M Barlogie, B Davies, F.E Morgan, G.J Weinhold, N |
author_facet | Rasche, L Alapat, D Kumar, M Gershner, G McDonald, J Wardell, C.P Samant, R Van Hemert, R Epstein, J Williams, A.F Thanendrarajan, S Schinke, C Bauer, M Ashby, C Tytarenko, R.G van Rhee, F Walker, B.A Zangari, M Barlogie, B Davies, F.E Morgan, G.J Weinhold, N |
author_sort | Rasche, L |
collection | PubMed |
description | The iliac crest is the sampling site for minimal residual disease (MRD) monitoring in Multiple Myeloma (MM). However, the disease distribution is often heterogeneous, and imaging can be used to complement MRD detection at a single site. We have investigated patients in complete remission (CR) during first-line or salvage therapy, for whom MRD flow-cytometry and the two imaging modalities positron-emission-tomography (PET) and diffusion-weighted magnetic resonance imaging (DW-MRI) were performed at the onset of CR. Residual focal lesions (FLs), detectable in 24% of first-line patients, were associated with short progression-free survival (PFS), with DW-MRI detecting disease in more patients. In some patients, FLs were only PET-positive, indicating that the two approaches are complementary. Combining MRD and imaging improved prediction of outcome, with double-negative and double-positive features defining groups with excellent and dismal PFS, respectively. FLs were a rare event (12%) in first-line MRD-negative CR patients. In contrast, patients achieving an MRD-negative CR during salvage therapy frequently had FLs (50%). Multi-region sequencing and imaging in an MRD-negative patient showed persistence of spatially separated clones. In conclusion, we show that DW-MRI is a promising tool for monitoring residual disease that complements PET and should be combined with MRD. |
format | Online Article Text |
id | pubmed-6586541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-65865412019-06-21 Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma Rasche, L Alapat, D Kumar, M Gershner, G McDonald, J Wardell, C.P Samant, R Van Hemert, R Epstein, J Williams, A.F Thanendrarajan, S Schinke, C Bauer, M Ashby, C Tytarenko, R.G van Rhee, F Walker, B.A Zangari, M Barlogie, B Davies, F.E Morgan, G.J Weinhold, N Leukemia Article The iliac crest is the sampling site for minimal residual disease (MRD) monitoring in Multiple Myeloma (MM). However, the disease distribution is often heterogeneous, and imaging can be used to complement MRD detection at a single site. We have investigated patients in complete remission (CR) during first-line or salvage therapy, for whom MRD flow-cytometry and the two imaging modalities positron-emission-tomography (PET) and diffusion-weighted magnetic resonance imaging (DW-MRI) were performed at the onset of CR. Residual focal lesions (FLs), detectable in 24% of first-line patients, were associated with short progression-free survival (PFS), with DW-MRI detecting disease in more patients. In some patients, FLs were only PET-positive, indicating that the two approaches are complementary. Combining MRD and imaging improved prediction of outcome, with double-negative and double-positive features defining groups with excellent and dismal PFS, respectively. FLs were a rare event (12%) in first-line MRD-negative CR patients. In contrast, patients achieving an MRD-negative CR during salvage therapy frequently had FLs (50%). Multi-region sequencing and imaging in an MRD-negative patient showed persistence of spatially separated clones. In conclusion, we show that DW-MRI is a promising tool for monitoring residual disease that complements PET and should be combined with MRD. 2018-12-20 2019-07 /pmc/articles/PMC6586541/ /pubmed/30573775 http://dx.doi.org/10.1038/s41375-018-0329-0 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Rasche, L Alapat, D Kumar, M Gershner, G McDonald, J Wardell, C.P Samant, R Van Hemert, R Epstein, J Williams, A.F Thanendrarajan, S Schinke, C Bauer, M Ashby, C Tytarenko, R.G van Rhee, F Walker, B.A Zangari, M Barlogie, B Davies, F.E Morgan, G.J Weinhold, N Combination of Flow Cytometry and Functional Imaging for Monitoring of Residual Disease in Myeloma |
title | Combination of Flow Cytometry and Functional Imaging for Monitoring
of Residual Disease in Myeloma |
title_full | Combination of Flow Cytometry and Functional Imaging for Monitoring
of Residual Disease in Myeloma |
title_fullStr | Combination of Flow Cytometry and Functional Imaging for Monitoring
of Residual Disease in Myeloma |
title_full_unstemmed | Combination of Flow Cytometry and Functional Imaging for Monitoring
of Residual Disease in Myeloma |
title_short | Combination of Flow Cytometry and Functional Imaging for Monitoring
of Residual Disease in Myeloma |
title_sort | combination of flow cytometry and functional imaging for monitoring
of residual disease in myeloma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586541/ https://www.ncbi.nlm.nih.gov/pubmed/30573775 http://dx.doi.org/10.1038/s41375-018-0329-0 |
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